Combating fungi with novel azolyl-tetrahydrofuran-2-ylidene-methanes

ABSTRACT

Azolyl-tetrahydrofuran-2-ylidene-methanes of the formula ##STR1## in which A represents a nitrogen atom or the CH group, 
     R represents alkyl, alkenyl, alkinyl, alkoxyalkyl, alkylthioalkyl, halogenoalkyl, halogenoalkoxyalkyl, halogenoalkylthioalkyl, halogenoalkenyl, optionally substituted aralkyl, optionally substituted aryloxyalkyl, optionally substituted arylthioalkyl, optionally substituted cycloalkyl or optionally substituted cycloalkylalkyl, 
     R 1  to R 6  are identical or different and represent hydrogen, alkyl, halogenoalkyl or halogen, up to at most 3 of the substituents representing halogen or halogenoalkyl, or 
     R 1  and R 2 , together with the carbon atom to which they are bonded, represent optionally substituted cycloalkyl, or 
     R 2  and R 3 , together with the carbon atoms to which they are bonded, represent optionally substituted cycloalkyl, 
     or addition products thereof with acids or metal salts. Some new intermediates are also shown.

The present invention relates to new substitutedazolyltetrahydrofuran-2-ylidene-methane derivatives, a process for theirpreparation and their use as fungicides.

It has already been disclosed that certain azolylalkenols, such as, forexample, 1-(imidazol-1-yl)- or1-(1,2,4-triazol-1-yl)-2-phenoxy-4,4-dimethyl-1-penten-3- have goodfungicidal properties (U.S. Pat. No. 4,360,528). It has also alreadybeen dislosed that disulphides, such as, for example, zincethylene-1,2-bisdithiocarbamidate, are good agents for combating fungalplant diseases (compare R. Wegler, "Chemie der Pflanzenschutz- undSchadlingsbekampfungsmittel" ("Chemistry of the Plant Protection Agentsand Agents for Combating Pests"), Volume 2, page 59 et seq.,Springer-Verlag 1970). However, the action of these compounds is notalways completely satisfactory in certain areas of indication, inparticular when low amounts and concentrations are applied. Newsubstituted azolyl-tetrahydrofuran-2-ylidene-methane derivatives of thegeneral formula (I) ##STR2## in which

A represents a nitrogen atom or the CH group,

R represents alkyl, alkenyl, alkinyl, alkoxyalkyl, alkylthioalkyl,halogenoalkyl, halogenoalkoxyalkyl, halogenoalkylthioalkyl,halogenoalkenyl, optionally substituted aralkyl, optionally substitutedaryloxyalkyl, optionally substituted arylthioalkyl, optionallysubstituted cycloalkyl or optionally substituted cycloalkylalkyl,

R¹ to R⁶ are identical or different and represent hydrogen, alkyl,halogenoalkyl or halogen, up to at most 3 of the substituentsrepresenting halogen or halogenoalkyl, or

R¹ and R², together with the carbon atom to which they are bonded,represent optionally substituted cycloalkyl, or

R² and R³, together with the carbon atoms to which they are bonded,represent optionally substituted cycloalkyl,

and acid addition salts and metal salt complexes thereof, have beenfound.

The compounds of the formula (I) can be in two geometric isomer forms,depending on the arrangement of the groups bonded to the double bond;they are preferentially obtained in a varying isomer ratio. The presentinvention relates both to the individual isomers and to the isomermixtures.

It has furthermore been found that the substitutedazolyl-tetrahydrofuran-2-ylidene-methane derivatives of the formula (I)are obtained by a process in whichazolyl(2-hydroxytetrahydrofuran-2-yl)-methane derivatives of the formula(II) ##STR3## in which

A, R and R¹ to R⁶ have the abovementioned meaning, are heated in thepresence of a diluent and in the presence of an acid catalyst, toseparate off water.

If appropriate, an acid or a metal salt can then be )added onto thecompounds of the formula (I) thus obtained.

It has also been found that the new substitutedazolyl-tetrahydrofuran-2-ylidene-methane derivatives of the formula (I)have powerful fungicidal properties. Surprisingly, the compounds of theformula (I) according to the invention exhibit better fungicidal actionsthan the 1-(imidazol-1-yl)- or1-(1,2,4-triazol-1-yl)-2-phenoxy-4,4-dimethyl-1-penten-3-ols which aresubstituted in the phenoxy part and are known from the prior art, andthan zinc ethylene-1,2-bisdithiocarbamidate, which is also known. Theactive compounds according to the invention thus represent an enrichmentof the art.

Formula (I) provides a general definition of the substitutedazolyl-tetrahydrofuran-2-ylidene-methane derivatives according to theinvention. Preferably, in this formula,

A represents a nitrogen atom or the CH group;

R represents straight-chain or branched alkyl with 1 to 12 carbon atoms,or represents straight-chain or branched alkenyl or alkinyl with in eachcase 2 to 12 carbon atoms, or represents straight-chain or branchedalkoxyalkyl or alkylthioalkyl with in each case 1 to 6 carbon atoms ineach alkyl part, or represents halogenoalkyl, halogenoalkoxyalkyl orhalogenoalkylthioalkyl with in each case 1 to 6 carbon atoms in eachalkyl part and with in each case 1 to 6 identical or different halogenatoms, such as fluorine and chlorine atoms, or representshalogenoalkenyl with 2 to 6 carbon atoms and 1 to 5 identical ordifferent halogen atoms, such as fluorine and chlorine atoms, orrepresents phenylalkyl, phenoxyalkyl or phenylthioalkyl with in eachcase 1 to 4 carbon atoms in the alkyl part and in each case optionallymonosubstituted or polysubstituted in the phenyl part by identical ordifferent substituents, substituents which may be mentioned being:halogen; alkyl, alkoxy and alkylthio with in each case 1 to 4 carbonatoms; halogenoalkyl, halogenoalkoxy and halogenoalkylthio with in eachcase 1 to 4 carbon atoms and 1 to 5 identical or different halogenatoms, such as fluorine and chlorine atoms; nitro; cyano; and optionallyhalogen-substituted phenyl and phenoxy; or represents cycloalkyl orcycloalkylalkyl with in each case 3 to 7 carbon atoms in the cycloalkylpart and 1 to 4 carbon atoms in the alkyl part and in each caseoptionally monosubstituted or polysubstituted by alkyl with 1 to 4carbon atoms;

R¹ to R⁶, which can be identical or different, represent hydrogen,straight-chain or branched alkyl with 1 to 4 carbon atoms, or representhalogenoalkyl with.1 or 2 carbon atoms and 1 to 5 identical or differenthalogen atoms, such as fluorine and chlorine atoms, up to a maximum of 3substituents representing halogenoalkyl,

R³ to R⁶, which can be identical or different, also represent halogen,up to a maximum of 3 substituents having this meaning; or

R¹ and R², together with the carbon atom to which they are bonded,represent cycloalkyl which has 4 to 7 carbon atoms and is optionallysubstituted by alkyl with 1 or 2 carbon atoms; or

R² and R³, together with the carbon atoms to which they are bonded,represent cycloalkyl which has 4 to 7 carbon atoms and is optionallysubstituted by alkyl with 1 or 2 carbon atoms.

Particularly preferred compounds of the formula (I) are those

in which

A represents a nitrogen atom or the CH group;

R represents straight-chain or branched alkyl with 1 to 8 carbon atoms,or represents straight-chain or branched alkenyl or alkinyl with in eachcase 2 to 6 carbon atoms, or represents straight-chain or branchedalkoxyalkyl or alkylthioalkyl with in each case 1 to 4 carbon atoms ineach alkyl part, or represents halogenoalkyl, halogenoalkoxyalkyl orhalogenoalkylthioalkyl with in each case 1 to a 4 carbon atoms in eachalkyl part and with in each case 1 to 5 fluorine and/or chlorine atoms,or represents halogenoalkenyl with 2 to 4 carbon atoms and 1 to 3fluorine and/or chlorine atoms; or represents phenylalkyl, phenoxyalkylor phenylthioalkyl with in each case 1 or 2 carbon atoms in the alkylpart and in each case optionally mono-, di- or tri-substituted in thephenyl part by identical or different substituents, substituents whichmay be mentioned being: fluorine, chlorine, methyl, ethyl, isopropyl,tert.-butyl, methoxy, methylthio, trifluoromethyl, trifluoromethoxy,trifluoromethylthio, nitro, cyano and optionally chlorine-substitutedphenyl and phenoxy; or represents cyclohexyl or cyclohexylmethyl, ineach case optionally substituted by methyl and/or ethyl;

R¹ to R⁶, which can be identical or different, represent hydrogen,methyl, ethyl or halogenomethyl with 1 to 3 identical or differenthalogen atoms, such as fluorine and chlorine atoms, a maximum of threesubstituents representing halogenomethyl; or

R³ to R⁶, which can be identical or different, also represent fluorine,chlorine or bromine, up to a maximum of three substituents having thismeaning; or

R¹ and R², together with the carbon atom to which they are bonded,represent cyclopentyl or cyclohexyl; or

R² and R³, together with the carbon atoms to which they are bonded,represent cyclopentyl or cyclohexyl.

The following compounds of the general formula (I) (wherein A representseither a nitrogen atom or the CH group) may be mentioned specifically,in addition to the compounds mentioned in the preparation examples:

    ______________________________________                                         ##STR4##                      (I)                                            R.sup.1                                                                              R.sup.2                                                                              R.sup.3                                                                             R.sup.4                                                                           R.sup.5                                                                           R.sup.6                                                                           R                                             ______________________________________                                        CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR5##                                     CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR6##                                     CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR7##                                     CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR8##                                     CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR9##                                     CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR10##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR11##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR12##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR13##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR14##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR15##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR16##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR17##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR18##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR19##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR20##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR21##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR22##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR23##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR24##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR25##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR26##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   CH.sub.2CCH                                   CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR27##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   CH.sub.2CH.sub.2CHCH.sub.2                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR28##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   CH.sub.3                                      CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H    C.sub.2 H.sub.5                              CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   C.sub.3 H.sub.7n                              CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   C.sub.5 H.sub.11n                             CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   C.sub.6 H.sub.13n                             CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H   C.sub.7 H.sub.15n                             CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR29##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR30##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR31##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR32##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR33##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR34##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR35##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR36##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR37##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR38##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR39##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR40##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR41##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR42##                                    CH.sub.3                                                                             CH.sub.3                                                                             H     H   H   H                                                                                  ##STR43##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR44##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR45##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR46##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR47##                                    C.sub.2 H.sub.5                                                                      CH     H     H   H   H                                                                                  ##STR48##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR49##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR50##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR51##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR52##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR53##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR54##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR55##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR56##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR57##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR58##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR59##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR60##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR61##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR62##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR63##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR64##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR65##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   CH.sub.2CCH                                   C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR66##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   CH.sub.2CH.sub.2CHCH.sub.2                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR67##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   CH.sub.3                                      C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   C.sub.2 H.sub.5                               C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   C.sub.3 H.sub.7n                              C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   C.sub.5 H.sub.11n                             C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   C.sub.6 H.sub.13n                             C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H   C.sub.7 H.sub.15n                             C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR68##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR69##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR70##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR71##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR72##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR73##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR74##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR75##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR76##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR77##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR78##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR79##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR80##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR81##                                    C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H     H   H   H                                                                                  ##STR82##                                    (CH.sub.2 ) .sub.5                                                                          H     H   H   H                                                                                  ##STR83##                                    (CH.sub.2 ) .sub.5                                                                          H     H   H   H   C.sub.4 H.sub.9                               (CH.sub.2 ) .sub.5                                                                          H     H   H   H                                                                                  ##STR84##                                    ______________________________________                                    

Addition products of acids and those substitutedazolyl-tetrahydrofuran-2-ylidene-methane derivatives of the formula (I)in which the substituents A, R and R¹ to R⁶ have the meanings which havealready been mentioned as preferred for these substituents are alsopreferred compounds according to the invention.

Preferred acids which can be added on include hydrogen halide acids,such as, for example, hydrochloric acid and hydrobromic acid, inparticular hydrochloric acid, and furthermore phosphoric acid, nitricacid, monofunctional and bifunctional carboxylic acids andhydroxycarboxylic acids, such as, for example, acetic acid, maleic acid,succinic acid, fumaric acid, tartaric acid, citric acid, salicylic acid,sorbic acid and lactic acid, and sulphonic acids, such asp-toluenesulphonic acid and 1,5-naphthalenedisulphonic acid.

Addition products of salts of metals of main groups II to IV and ofsub-groups I and II and IV to VIII and those substitutedazolyl-tetrahydrofuran-2-ylidene-methane derivatives of the formula (I)in which the substituents A, R and R¹ to R⁶ have the meanings which havealready been mentioned as preferred for these substituents are alsopreferred compounds according to the invention.

Salts of copper, zinc, manganese, magnesium, tin, iron and nickel areparticularly preferred here. Possible anions of these salts are thosewhich are derived from acids which lead to physiologically acceptableaddition products. In this connection, particularly preferred acids ofthis type are the hydrogen halide acids, such as, for example,hydrochloric acid and hydrobromic acid, nitric acid and sulphuric acid.

If, for example,1-(4-chlorophenyl)-2-(3,3-dimethyl-2-hydroxy-tetrahydrofuran-2-yl)-2-(1,2,4-triazol-1-yl)-ethaneis used as the starting substance, the course of the reaction in theprocess according to the invention can be represented by the followingequation: ##STR85##

Formula (II) provides a general definition of theazolyl-(2-hydroxytetrahydrofuran-2-yl)-methane derivatives to be used asstarting substances in carrying out the process according to theinvention. In this formula, A, R and R¹ to R⁶ preferably represent theradicals which have already been mentioned as preferred for thesesubstituents in connection with the description of the substances of theformula (I) according to the invention.

The azolyl-(2-hydroxy-tetrahydrofuran-2-yl)-methane derivatives of theformula (II) are not yet known; they are obtained by a process in which

(a) 2-azolylmethyl-2-hydroxy-tetrahydrofurans of the formula ##STR86##in which

A and R¹ to R⁶ have the abovementioned meaning, are reacted with analkylating agent of the formula (IV)

    Z--R                                                       (IV)

in which

R has the abovementioned meaning and

Z represents an electron-withdrawing leaving grouping, such as, forexample, p-methylphenysulphonyloxy, the grouping -0-SO₂ -OR' or -NR₃ 'or the like,

wherein

R' represents, for example, an optionally substituted hydrocarbonradical,

in the presence of a diluent and in the presence of a base.

Possible diluents for process (a) are inert organic solvents. Theseinclude, preferably, aromatic hydrocarbons, such as benzene, toluene orxylene; halogenated hydrocarbons, such as methylene chloride, carbontetrachloride, chloroform or chlorobenzene; esters, such as ethylacetate; formamides, such as dimethylformamide; and dimethylsulphoxide.

Process (a) is carried out in the presence of a base. All the customaryorganic and, in particular, inorganic bases can be used here, such as,preferably, alkali metal hydroxides or alkali metal carbonates, sodiumhydroxide and potassium hydroxide being mentioned as examples..

The reaction temperatures can be varied within a substantial range incarrying out process (a). In general, the reaction is carried outbetween 0° and 100° C., preferably between 20° and 100° C.

In carrying out process (a), 1 to 1.2 moles of alkylating agent arepreferably employed per mole of the compound of the formula (III). Theintermediates of the formula (II) are isolated in a generally customarymanner.

Process (a) can also be carried out in a two-phase system, such as, forexample, aqueous sodium hydroxide solution or potassium hydroxidesolution/toluene or methylene chloride, if appropriate with addition of0.1 to 1 mole of a phase transfer catalyst, such as, for example,ammonium or phosphonium compounds, examples which may be mentioned beingbenzyldodecyldimethyl-ammonium chloride and triethyl-benzyl-ammoniumchloride.

The 2-azolylmethyl-2-hydroxy-tetrahydrofurans of the formula (III) to beused as starting substances for process (a) are likewise not yet known;they are obtained by a process in which

(b) water is added onto 2-azolylmethylene-tetrahydrofurans of theformula (V) ##STR87## in which A and R¹ to R⁶ have the abovementionedmeaning, in the presence of a diluent and in the presence of an acid asa catalyst.

Possible diluents for process (b) are water-miscible solvents. Theseinclude, preferably, alcohols, such as methanol or ethanol; ketones,such as acetone; and water.

Process (b) is carried out in the presence of an acid as a catalyst. Allthe customary organic and inorganic acids can be employed here, such as,preferably, sulphuric acid, hydrochloric acid, nitric acid,methanesulphonic acid and p-toluenesulphonic acid.

The reaction temperatures can be varied within a substantial range incarrying out process (b). In general, the reaction is carried outbetween 0° and 100° C., preferably between 20° and 80° C.

The alkylating agents of the formula (IV) also to be used as startingsubstances for process (a) are generally known compounds of organicchemistry.

Some of the 2-azolylmethylene-tetrahydrofurans of the formula (V) to beused as starting substances for process (b) are known (U.S. Ser. No.461,369 filed Jan. 27, 1983, now U.S. Pat. No. 4,487,776, correspondingto German Published Specification No. 3,204,795). The2-azolylmethylene-tetrahydrofurans of the formula (Va) are not yetknown. ##STR88## in which

A and R³ to R⁶ have the abovementioned meaning and

R^(1') and R^(2') represent the abovementioned meanings of R¹ and,respectively, R², the two radicals not simultaneously representingmethyl if R³ to R⁶ simultaneously represent hydrogen.

The 2-azolylmethylene-tetrahydrofurans of the formula (V) or (Va) areobtained by a process in which (c) halogenoketones of the formula (VI)##STR89## in which R¹ to R⁶ have the abovementioned meaning and Hal andHal' represent halogen, preferably chlorine or bromine, are reacted withazoles of the formula (VII) ##STR90## in which A has the abovementionedmeaning, in the presence of a diluent and in the presence of anacid-binding agent.

Possible diluents for process (c) are inert organic solvents. Theseinclude, preferably, ketones, such as diethyl ketone and, in particular,acetone and methyl ethyl ketone; nitriles, such as propionitrile, inparticular acetonitrile; alcohols, such as ethanol or isopropanol;ethers, such as tetrahydrofuran or dioxane; aromatic hydrocarbons, suchas toluene, benzene or chlorobenzene; formamides, such as, inparticular, dimethylformamide; and halogenated hydrocarbons.

Process (c) is carried out in the presence of an acid-binding agent. Allthe inorganic or organic acid-binding agents which can customarily beused may be added, such as alkali metal carbonates, for example sodiumcarbonate, potassium carbonate and sodium bicarbonate, or such as lowertertiary alkylamines, cycloalkylamines or aralkylamines, for exampletriethylamine, N,N-dimethylcyclohexylamine, dicyclohexylamine andN,N-dimethylbenzylamine, and furthermore pyridine anddiazabicyclooctane.

An appropriate excess of azole is preferably used.

The reaction temperatures can be varied within a substantial range incarrying out process (c). In general, the reaction is carried outbetween about 20° and 150° C., preferably at 60° to 120° C.

In carrying out process (c), 1 to 4 moles of azole of the formula (VII)and 1 to 4 moles of acid-binding agent are preferably employed per moleof the compounds of the formula (VI). The compounds of the formula (V)or (Va) are isolated in the customary manner.

Some of the halogenoketones of the formula (VI) to be used as startingsubstances for process (c) are known (U.S. Ser. No. 460,687 filed Jan.24, 1983, now abandoned corresponding to German Published SpecificationNo. 3,204,788). The halogenoketones of the formula (VIa) ##STR91## inwhich Hal, Hal', R³ to R⁶, R^(1') and R^(2') have the abovementionedmeaning, are not yet known.

The halogenoketones of the formula (VI) or (VIa) are obtained by aprocess in which (d) 2-chloromethylene-tetrahydrofurans of the formula(VIII) ##STR92## in which R¹ to R⁶ have the abovementioned meaning, arereacted with acid compounds of the formula (IX)

    H--Hal                                                     (IX)

in which Hal has the abovementioned meaning, if appropriate in thepresence of a diluent.

Possible diluents for process (d) are inert organic solvents. Theseinclude, preferably, aromatic hydrocarbons, such as toluene, benzene orchlorobenzene; formamides, such as dimethylformamide; nitriles, such asacetonitrile; and halogenated hydrocarbons, such as methylene chloride.

The reaction temperatures can be varied within a substantial range incarrying out process (d). In general, the reaction is carried outbetween 0° and 150° C.; preferably at 10° to 120° C.

Certain halogenoketones of the formula (VI) or (VIa) can also beobtained by reacting correspondingly substituted ketones or unsaturatedketones with halogenating agents, such as, for example, bromine,hydrogen bromide or sulphuryl chloride, in the customary manner (in thiscontext, compare also the preparation examples).

The azoles of the formula (VII) also to be used as starting substancesfor process (c) are generally known compounds of organic chemistry.

Some of the 2-chloromethylene-tetrahydrofurans of the formula (VIII) tobe used as starting substances for process (d) are known (compare DE-OS(German Published Specification) No. 3,204,692). The2-chloromethylene-tetrahydrofurans of the formula (VIIIa) ##STR93## inwhich R^(1'), R^(2') and R³ to R⁶ have the abovementioned meaning, arenot yet known.

The 2-chloromethylene-tetrahydrofurans of the formula (VIII) or (VIIIa)are obtained by a process in which, for example,

(e) 1,1,5-trichloro-pentene derivatives of the formula (X) ##STR94## inwhich R¹ to R⁶ have the abovementioned meaning, or1,1,1,5-tetrachloro-pentane derivatives of the formula (XI) ##STR95## inwhich R¹ to R⁶ have the abovementioned meaning, are reacted withcarboxylates, such as, in particular, anhydrous sodium acetate, and withbases, such as, in particular, alkali metal alcoholates, in the presenceof a diluent.

Possible diluents for process (e) are inert organic solvents. Theseinclude, preferably, formamides, such as dimethylformamide; nitriles,such as acetonitrile; and halogenated hydrocarbons.

The reaction temperatures can be varied within a substantial range incarrying out process (e). In general, the reaction is carried outbetween 20° and 150° C., preferably at the boiling point of the solventused.

In carrying out process (e), 1 to 2 moles of carboxylate and 1 to 2moles of base are preferably employed per mole of the compounds of theformulae (X) or (XI). The desired products are isolated in the customarymanner.

The acid compounds of the formula (IX) to be used as starting substancesfor process (d) according to the invention are generally known compoundsof organic chemistry.

The compounds of the formula (X) or (XI) to be used as startingsubstances for process (e) are known compounds of organic chemistry, orthey can be obtained in a known manner.

Possible diluents for the reaction according to the invention are inertorganic solvents. These include, preferably, aromatic hydrocarbons, suchas toluene, benzene, xylene, chlorobenzene or dichlorobenzene; andhalogenated aliphatic hydrocarbons, such as dichloroethane.

The reaction according to the invention is carried out in the presenceof an acid catalyst. Acid catalysts include, preferably, aliphatic andaromatic sulphonic acids, such as p-toluenesulphonic acid ormethanesulphonic acid, which may also optionally be in polymer-bondedform.

The reaction temperatures can be varied within a substantial range inthe reaction according to the invention. In general, the reaction iscarried out between about 50° and 150° C., preferably at 80° to 120° C.

In carrying out the reaction according to the invention, catalyticamounts of acid catalyst are employed per mole of the compounds of theformula (II). The compounds of the formula (I) are isolated in thecustomary manner.

The acid addition salts of the compounds of the formula (I) can beobtained in a simple manner by customary salt formation methods, forexample by dissolving a compound of the formula (I) in a suitable inertsolvent and adding the acid, for example hydrochloric acid, and, ifappropriate, purified by washing with an organic solvent.

The metal salt complexes of the compounds of the formula (I) can beobtained in a simple manner by customary processes, thus, for example,by dissolving the metal salt in alcohol, for example ethanol, and addingthe solution to the compounds of the formula (I). The metal saltcomplexes can be purified in a known manner, for example by filtration.

The active compounds according to the invention exhibit a powerfulmicrobicidal action and can be employed in practice for combatingundesired micro-organisms. The active compounds are suitable for use asplant protection agents.

Fungicidal agents in plant protection are employed for combatingPlasmodiophoromycetes, Oomycetes, Chytridiomycetes, Zygomycetes,Ascomycetes, Basidiomycetes and Deuteromycetes.

The good toleration, by plants, of the active compounds, at theconcentrations required for combating plant diseases, permits treatmentof above-ground parts of plants, of vegetative propagation stock andseeds, and of the soil.

As plant protection agents, the active compounds according to theinvention can be used with particularly good success for combatingSphaerotheca species, such as against the powdery mildew of barleycausative organism (Sphaerotheca fuliginea); Botrytis species, such asagainst the grey mould causative organism (Botrytis cinerea); cerealdiseases, such as Erysiphe graminis, rusts, Septoria, Cochliobolussativus, Pyrenophora teres or Pyrenophora graminea; and rice diseases,such as Pyricularia oryzae and Pellicularia sasakii. The substancesaccording to the invention also exhibit a broad and good in vitrofungicidal action spectrum.

It should be emphasized that the substances according to the inventionnot only have a protective action but in some cases are also systemic.Thus, it is possible to protect plants from fungal attack if the activecompound is fed to the above-ground parts of the plant via the soil andthe root or via the seed.

The active compounds can be converted to the customary formulations,such as solutions, emulsions, wettable powders, suspensions, powders,dusts, foams, pastes, soluble powders, granules, aerosols,suspension-emulsion concentrates, seed treatment powders, natural andsynthetic materials impregnated with active compounds, very finecapsules in polymeric substances and in coating compositions for seed,and formulations used with burning equipment, such as fumigatingcartridges, fumigating cans, fumigating coils and the like, as well asULV cold mist and warm mist formulations.

These formulations are produced in known manner, for example by mixingthe active compounds with extenders, that is, liquid solvents, liquefiedgases under pressure, and/or solid carriers, optionally with the use ofsurface-active agents, that is, emulsifying agents and/or dispersingagents, and/or foam-forming agents. In the case of the use of water asan extender, organic solvents can, for example, also be used asauxiliary solvents. As liquid solvents, there are suitable in the main:aromatics, such as xylene, toluene or alkyl naphthalenes, chlorinatedaromatics or chlorinated aliphatic hydrocarbons, such as chlorobenzenes,chloroethylenes or methylene chloride, aliphatic hydrocarbons, such ascyclohexane or paraffins, for example mineral oil fractions, alcohols,such as butanol or glycol as well as their ethers and esters, ketones,such as acetone, methyl ethyl ketone, methyl isobutyl ketone orcyclohexanone, strong polar solvents, such as dimethylformamide anddimethyl sulphoxide, as well as water; by liquefied gaseous extenders orcarriers are meant liquids which are gaseous at normal temperature andunder normal pressure, for example aerosol propellants, such ashalogenated hydrocarbons as well as butane, propane, nitrogen and carbondioxide; as solid carriers there are suitable: for example groundnatural minerals, such as kaolins, clays, talc, chalk, quartz,attapulgite, montmorillonite or diatomaceous earth, and ground syntheticminerals, such as highly-dispersed silicic acid, alumina and silicates;as solid carriers for granules there are suitable: for example crushedand fractionated natural rocks such as calcite, marble, pumice,sepiolite and dolomite, as well as synthetic granules of inorganic andorganic meals, and granules of organic material such as sawdust, coconutshells, corn cobs and tobacco stalks; as emulsifying and/or foam-formingagents there are suitable: for example non-ionic and anionicemulsifiers, such as polyoxyethylene-fatty acid esters,polyoxyethylene-fatty alcohol ethers, for example alkylaryl polyglycolethers, alkyl sulphonates, alkyl sulphates, aryl sulphonates as well asalbumin hydrolysis products; as dispersing agents there are suitable:for example ligninsulphite waste liquors and methylcellulose.

Adhesives such as carboxymethylcellulose and natural and syntheticpolymers in the form of powders, granules or latices, such as gumarabic, polyvinyl alcohol and polyvinyl acetate, as well as naturalphospholipids, such as cephalins and lecithins, and syntheticphospholipids, can be used in the formulations. Other additives can bemineral and vegetable oils.

It is possible to use colorants such as inorganic pigments, for exampleiron oxide, titanium oxide and Prussian Blue, and organic dyestuffs,such as alizarin dyestuffs, azo dyestuffs and metal phthalocyaninedyestuffs, and trace nutrients such as salts of iron, manganese, boron,copper, cobalt, molybdenum and zinc.

The formulations in general contain between 0.1 and 95 per cent byweight of active compound, preferably between 0.5 and 90%.

The active compounds according to the invention can be present in theformulations or in the various use forms as a mixture with other knownactive compounds, such as fungicides, bactericides, insecticides,acaricides, nematicides, herbicides, bird repellents, growth factors,plant nutrients and agents for improving soil structure.

The active compounds can be used as such or in the form of theirformulations or the use forms prepared therefrom by further dilution,such as ready-to-use solutions, emulsions, suspensions, powders, pastesand granules. They are used in the customary manner, for example bywatering, immersion, spraying, atomizing, misting, vaporizing,injecting, forming a slurry, brushing on, dusting, scattering, drydressing, moist dressing, wet dressing, slurry dressing or encrusting.

In the treatment of parts of plants, the active compound concentrationsin the use forms can be varied within a substantial range. They are, ingeneral, between 1 and 0.0001% by weight, preferably between 0.5 and0.001%.

In the treatment of seed, amounts of active compound of 0.001 to 50 gper kilogram of seed, preferably 0.01 to 10 g, are generally required.

For the treatment of soil, active compound concentrations of 0.00001 to0.1% by weight, preferably 0.0001 to 0.02% by weight, are required atthe place of action.

Preparation Examples Example 1 and 2 ##STR96##

Example-(I-1)=form A

Example (I-2)=form B

(Form A and form B=the two possible geometric isomers)

5 g (0.0155 mole) of1-(4-chlorophenyl)-2-(3,3-dimethyl-2-hydroxy-tetrahydrofuran-2-yl)-2-(1,2,4-triazol-1-yl)-ethane are dissolved in 100 ml of toluene, 0.5 g ofp-toluenesulphonic acid are added and the mixture is heated under refluxfor 2 hours, using a water separator. The reaction mixture is cooled,washed with water, dried over sodium sulphate and concentrated in vacuo.The residue is purified by column chromatography (silica gel; ethylacetate/cyclohexane=3:1). 2.8 g (59.6% of theory) of1-(4-chlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneare obtained as form A of melting point 89° C. and 0.4 g (8.5% oftheory) of1-(4-chlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneare obtained as form B of melting point 175-177° C.

Preparation of the starting substance ##STR97##

10.3 g (0.052 mole) of3,3-dimethyl-2-hydroxy-2-(1,2,4-triazol-1-yl-methyl)-tetrahydrofuran,2.9 g (0.052 mole) of potassium hydroxide and 8.4 g (0.052 mole) of4-chlorobenzyl chloride are stirred in a mixture of 100 ml ofdimethylsulphoxide and 6 ml of water at 30° C. for 2 hours. The reactionsolution is then poured onto water and extracted with ethyl acetate. Theorganic phase is dried over sodium sulphate and concentrated. Aftertrituration in n-hexane, the residue crystallizes. 6.6 g (39.5% oftheory) of1-(4-chlorophenyl)-2-(3,3-dimethyl-2-hydroxy-tetrahydrofuran-2-yl)-2-(1,2,4-triazol-1-yl)-ethaneof melting point 98° C. are obtained. ##STR98##

30 g (0.17 mole) of(3,3-dimethyl-tetrahydrofuran-2-ylidene)-(1,2,4-triazol-1-yl)-methaneand 100 g of concentrated hydrochloric acid are stirred in 300 ml ofmethanol at room temperature for 4 hours. The reaction mixture isconcentrated in vacuo, the residue is taken up in water, the pH value isadjusted to 7 to 8 with dilute sodium hydroxide solution and the mixtureis extracted with methylene chloride. The organic phase is washed withwater, dried over sodium sulphate and concentrated in vacuo. 30.7 g (93%of theory) of3,3-dimethyl-2-hydroxy-2-(1,2,4-triazol-1-yl-methyl)-tetrahydrofuran ofmelting point 93°-95° C. are obtained. ##STR99##

85 g (1.23 moles) of 1,2,4-triazole and 464 g (33.6 moles) of potassiumcarbonate are initially introduced into 2.5 liters of acetone. 220 g(1.12 moles) of 1,5-dichloro-3,3-dimethyl-2-pentanone are added dropwiseat room temperature, without cooling and with stirring. When theaddition has ended, the mixture is subsequently stirred at the refluxtemperature for 2 hours.

The reaction mixture is cooled and filtered over a suction filter andthe mother liquor is concentrated in vacuo. The residue is taken up inmethylene chloride and the mixture is washed with water, dried oversodium sulphate and concentrated. The residue is stirred in petroleumether, filtered off with suction and dried at 50° C. in vacuo. 145.3 g(56.5% of theory) of (3,3-dimethyl-tetraLehydrofuran-2-ylidene)-(1,2,4-triazol-1-yl)-methane of melting point 47°C. are obtained. ##STR100##

A powerful stream of hydrogen chloride gas from a cylinder is passedinto 476 g (3.25 moles) of2-chloromethylene-3,3-dimethyltetrahydrofuran, with ice-cooling. The gasis absorbed completely and the internal temperature rises up to 30° C.After complete saturation with hydrogen chloride, the reaction mixtureis subsequently stirred at room temperature for 2 hours. Excess hydrogenchloride is initially stripped off using a water pump, and the mixtureis then distilled under a high vacuum. 531 g (90% of theory) of1,5-dichloro-3,3-dimethyl-2-pentanone of boiling point 85°-90° C./0.3mbar are obtained. ##STR101##

806 g (4 moles) of 1,1,5-trichloro-3,3-dimethyl-1-pentene are heatedunder reflux with 360 g (4.4 moles) of anhydrous sodium acetate in 1liter of dimethylformamide for 6 hours. After cooling to about 100° C.,1.6 liters (8 moles) of 30% strength sodium methylate solution inmethanol are added dropwise and the mixture is heated under reflux for afurther 4 hours. The cold solution is poured into water and extractedseveral times with methylene chloride. After the solution has been driedand the solvent has been distilled off, 654 g of product remain, and arefractionated over a column. 522 g (89% of theory) of2-chloromethylene-3,3-dimethyl-tetrahydrofuran of boiling point 84°-87°C./20 mbar are obtained.

The following end products of the general formula ##STR102## areobtained in a corresponding manner according to the process conditionsdescribed:

    __________________________________________________________________________    Example                            m.p. (°C.)                          No.  R.sup.1                                                                          R.sup.2                                                                          R.sup.3                                                                         R.sup.4                                                                         R.sup.5                                                                         R.sup.6                                                                         R            A  or n.sub.D.sup.20                          __________________________________________________________________________    I-3  C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR103##  N  1,5607 (Form A)                            I-4  C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR104##  N  78 (Form B)                                I-5  CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR105##  N  69-70 (Form A)                             I-6  CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR106##  N  106 (Form B)                               I-7  CH.sub.3                                                                         CH.sub.3                                                                         H H H H C.sub.4 H.sub.9                                                                            N  1,4959                                                                        (Form A)                                   I-8  CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR107##  N  1,5158 (Form A)                            I-9  CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR108##  N  118                                        I-10 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR109##  CH 1,5616                                     I-11 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR110##  CH 1,5672                                     I-12 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR111##  CH 1,5429                                     I-13 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR112##  CH 1,5530                                     I-14 CH.sub.3                                                                         CH.sub.3                                                                         H H H H C.sub.4 H.sub.9                                                                            CH 1,5016                                     I-15 CH.sub.3                                                                         CH.sub.3                                                                         H H H H CH.sub.2CHCH.sub.2                                                                         CH 1,5163                                     I-16 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR113##  N  70-75 (Form A)                             I-17 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR114##  N  60-65                                      I-18 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR115##  CH 1,5574                                     I-19 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR116##  CH 1,5441                                     I-20 CH.sub.3                                                                         C.sub.2 H.sub.5                                                                  H H H H                                                                                ##STR117##  CH 1,5726                                     I-21 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR118##  N  1,5471                                     __________________________________________________________________________     Form A and Form B = the two possible geometric isomers                   

The following starting substances of the formula ##STR119## can beotained according to Example 1 and the process conditions described:

    __________________________________________________________________________    Example                            m.p.(°C.)                           NO.  R.sup.1                                                                          R.sup.2                                                                          R.sup.3                                                                         R.sup.4                                                                         R.sup.5                                                                         R.sup.6                                                                         R            A  or n.sub.D.sup.20                          __________________________________________________________________________    II-2 CH.sub.3                                                                         CH.sub.3                                                                         H H H H C.sub.4 H.sub.9                                                                            N  1.4888                                     II-3 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR120##  N  109                                        II-4 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR121##  N  123-25                                     II-5 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR122##  N  1.5349                                     II-6 C.sub.2 H.sub.5                                                                  CH.sub.3                                                                         H H H H                                                                                ##STR123##  N  1.5368                                     II-7 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR124##  CH 130-32                                     II-8 CH.sub.3                                                                         CH.sub.3                                                                         H H H H C.sub.4 H.sub.9                                                                            CH 1.4913                                     II-9 CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR125##  CH 164                                        II-10                                                                              CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR126##  CH 144-45                                     II-11                                                                              CH.sub.3                                                                         CH.sub.3                                                                         H H H H CH.sub.2CHCH.sub.2                                                                         CH 1.5065                                     II-12                                                                              CH.sub.3                                                                         CH.sub.3                                                                         H H H H                                                                                ##STR127##  CH 135-36                                     __________________________________________________________________________

The following starting substances of the formula (III) ##STR128## can beobtained according to Example 1 and the process conditions described:

    ______________________________________                                        Example                                                                       No.    R.sup.1                                                                              R.sup.2 R.sup.3                                                                           R.sup.4                                                                            R.sup.5                                                                            R.sup.6                                                                            A    m.p. (°C.)               ______________________________________                                        III-2  C.sub.2 H.sub.5                                                                      CH.sub.3                                                                              H   H    H    H    N    88                              III-3  CH.sub.3                                                                             CH.sub.3                                                                              H   H    H    H    CH   107-08                          ______________________________________                                    

The following starting substances of the formula (Va) ##STR129## can beobtained according to Example 1 and the process conditions described:

    ______________________________________                                        Example                                                                       No.    R.sup.1 '                                                                            R.sup.2 '                                                                            R.sup.3                                                                            R.sup.4                                                                           R.sup.5                                                                              R.sup.6                                                                            A    n.sub.D.sup.20                 ______________________________________                                        Va-1   CH.sub.3                                                                             CH.sub.3                                                                             H    H   CH.sub.3                                                                             H    N    1.5219                         Va-2   C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H    H   H      H    N    1.5237                         Va-3   CH.sub.3                                                                             CH.sub.3                                                                             H    H   --CH.sub.2 Br                                                                        H    N    1.5452                         Va-4   C.sub.2 H.sub.5                                                                      CH.sub.3                                                                             H    H   H      H    CH   1.5364                         ______________________________________                                    

The following examples demonstrate further possibilities of thepreparation of starting substances of the formula (VI) or (VIa):

EXAMPLE a ##STR130##

170.7 g (1.066 moles) of bromine are added dropwise to 67.2 g (0.533mole) of 3,3-dimethyl-5-hexen-2-one in 500 ml of chloroform at roomtemperature. The mixture is subsequently stirred for 30 minutes, washedwith water, dried over sodium solphate and concentrated in vacuo. 188 g(96.5% of theory) of 3,3-dimethyl-1,5,6-tribromo-2-hexanone ofrefractive index n²⁰ _(?) =1.5387 are obtained.

EXAMPLE b ##STR131##

20.9 g (0.13 mole) of bromine are added dropwise to 27 g (0.13 mole) of5-bromo-3,3-dimethyl-2-hexanone in 50 ml chloroform at room temperature.The mixture is subsequently stirred at room temperature for 30 minutes,washed with water, dried over sodium sulphate and concentrated in vacuo.36.9 g (99% of theory) of 1,5-dibromo-3,3-dimethyl-2-hexanone ofrefractive index n²⁰ _(?) =1.5015 are obtained.

Preparation of the intermediate ##STR132##

18.9 g (0.15 mole) of 3,3-dimethyl-5-hexen-2-one and 1.6 g (0.0054 mole)of iron-III bromide are dissolved in 150 ml of chloroform. 0.16 mole ofhydrogen bromide gas are passed in at 0° C. in the course of 90 minutes.The mixture is subsequently stirred at room temperature for 2 hours andthe organic phase is separated off, washed with water, dried over sodiumsulphate and concentrated in vacuo. 27 g (87% of theory) of5-bromo-3,3-dimethyl-2-hexanone of refractive index n_(D) ²⁰ =1.4639 areobtained.

USE EXAMPLES

The compounds shown below are used as comparison substances in the useexamples which follow: ##STR133##

EXAMPLE A

Botrytis test (bean)/protective

Solvent: 4.7 parts by weight of acetone

Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amounts of solvent andemulsifier, and the concentrate is diluted with water to the desiredconcentration.

To test for protective activity, young plants are sprayed with thepreparation of active compound until dripping wet. After the spraycoating has dried on, 2 small pieces of agar covered with Botrytiscinerea are placed on each leaf. The inoculated plants are placed in adarkened humidity chamber at 20° C. 3 days after the inoculation, thesize of the infected spots on the leaves is evaluated.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:1, 6, 10, 16 and 17.

EXAMPLE B

Sphaerotheca test (cucumber) / protective

Solvent: 4.7 parts by weight of acetone

Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amounts of solvent andemulsifier, and the concentrate is diluted with water to the desiredconcentration.

To test for protective activity, young plants are sprayed with thepreparation of active compound until dripping wet. After the spraycoating has dried on, the plants are dusted with conidia of the fungusSphaerotheca fuliginea.

The plants are then placed in a greenhouse at 23° to 24° C. and at arelative atmospheric humidity of about 75%.

Evaluation is carried out 10 days after the inoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:5 and 6.

EXAMPLE C

Pyricularia test (rice)/protective

Sovent: 12.5 parts by weight of acetone

Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent, and theconcentrate is diluted with water and the stated amount of emulsifier,to the desired concentration.

To test for protective activity, young rice plants are sprayed with thepreparation of active compound until dripping wet. After the spraycoating has dried on, the plants are inoculated with an aqueous sporesuspension of Pyricularia oryzae. The plants are then placed in agreenhouse at 100% relative atmospheric humidity and 25° C.

Evaluation of the disease infestation is carried out 4 days after theinoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:1, 9, 12 and 11.

EXAMPLE D

Pyricularia test (rice)/systemic

Solvent: 12.5 parts by weight of acetone

Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amounts of solvent, and theconcentrate is diluted with water and the stated amount of emulsifier,to the desired concentration.

To test for systemic properties, standard soil in which young riceplants have been grown is watered with 40 ml of the preparation ofactive compound. 7 days after the treatment, the plants are inoculatedwith an aqueous spore suspension of Pyricularia oryzae. Thereafter, theplants remain in a greenhouse at a temperature of 25° C. and a relativeatmospheric humidity of 100% until they are evaluated.

Evaluation of the disease infestation is carried out 4 days after theinoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:1, 9, 14 and 12.

EXAMPLE E

Pellicularia test (rice)

Solvent: 12.5 parts by weight of acetone

Emulsifier: 0.3 parts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amount of solvent, and theconcentrate is diluted with water and the stated amount of emulsifier,to the desired concentration.

To test for activity, young rice plants in the 3 to 4 leaf stage aresprayed until dripping wet. The plants remain in a greenhouse until theyhave dried off. The plants are then inoculated with Pellicularia sasakiiand are placed at 25° C. and 100% relative atmospheric humidity.

The evaluation of the disease infestation is carried out 5 to 8 daysafter the inoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:1, 9, 14, 12 and 11.

EXAMPLE F

Erysiphe test (barley)/protective

Solvent: 100 parts by weight of dimethylformamide

Emulsifier: 0.25 arts by weight of alkylaryl polyglycol ether

To produce a suitable preparation of active compound, 1 part by weightof active compound is mixed with the stated amounts of solvent andemulsifier, and the concentrate is diluted with water to the desiredconcentration.

To test for protective activity, young plants are sprayed with thepreparation of active compound until dew-moist. After the spray coatinghas dried on, the plants are dusted with spores of Erysiphe graminisf.sp. hordei.

The plants are placed in a greenhouse at a temperature of about 20° C.and a relative atmospheric humidity of about 80%, in order to promotethe development of powdery mildew pustules.

Evaluation is carried out 7 days after the inoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:1, 5, 10, 11 and 12.

EXAMPLE G

Erysiphe test (barley)/seed treatment

The active compounds are used as dry dressings. These are prepared byextending the particular active compound with a ground mineral to give afinely pulverulent mixture, which ensures uniform distribution on theseed surface.

To apply the dressing, the seed is shaken with the dressing in a closedglass flask for 3 minutes.

3 batches of 12 grains of the barley are sown 2 cm deep in standardsoil. 7 days after sowing, when the young plants have unfolded theirfirst leaf, they are dusted with spores of Erysiphe graminis f.sp.hordei.

The plants are placed in a greenhouse at a temperature of about 20° C.and a relative atmospheric humidity of about 80% in order to promote thedevelopment of powdery mildew pustules.

Evaluation is carried out 7 days after the inoculation.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compound according to preparation example: 1.

EXAMPLE H

Drechslera graminea test (barley)/seed treatment (syn. Helminthosporiumgramineum)

The active compounds are used as dry dressings. These are prepared byextending the particular active compound with a ground mineral to give afinely pulverulent mixture, which ensures uniform distribution on theseed surface.

To apply the dressing, the infected seed is shaken with the dressing ina closed glass flask for 3 minutes.

The seed is embedded in sieved, moist standard soil and is exposed to atemperature of 4° C. in closed Petri dishes in a refrigerator for 10days. Germination of the barley, and possibly also of the fungus spores,is thereby initiated. 2 batches of 50 grains of the pregerminated barleyare subsequently sown 3 cm deep in standard soil and are cultivated in agreenhouse at a temperature of about 18° C., in seedboxes which areexposed to light for 15 hours daily.

About 3 weeks after sowing, the plants are evaluated for symptoms ofstripe disease.

In this test, a clearly superior activity compared with the prior art isshown, for example, by the compounds according to preparation examples:14 and 10.

It will be understood that the specification and examples areillustrative but not limitative of the present invention and that otherembodiments within the spirit and scope of the invention will suggestthemselves to those skilled in the art.

We claim:
 1. An azolyl-tetrahydrofuran-2-ylidene-methane derivative ofthe formula ##STR134## in which A represents a nitrogen atom or the CHgroup,R represents straight-chain or branched alkyl with 1 to 12 carbonatoms, or represents straight-chain or branched alkenyl or alkinyl within each case 2 to 12 carbon atoms, or represents straight-chain orbranched alkoxyalkyl or alkylthioalkyl with in each case 1 to 6 carbonatoms in each alkyl part, or represents halogenoalkenyl,halogenoalkoxyalkyl or halogenoalkylthioalkyl with in each case 1 to 6carbon atoms in each alkyl part and with in each case 1 to 6 identicalor different halogen atoms or represents halogenoalkenyl with 2 to 6carbon atoms and 1 to 5 identical or different halogen atoms, orrepresents phenylakyl, phenoxyalkyl or phenylthioalkyl with in each case1 to 4 carbon atoms in the alkyl part and in each case optionallymonosubstituted or polysubstituted in the phenyl part by identical ordifferent substituents selected from the group consisting of halogen,alkyl, alkoxy and alkylthio with in each case 1 to 4 carbon atoms;halogenoalkyl, halogenoalkoxy and halogenoalkylthio with in each case 1to 4 carbon atoms and 1 to 5 identical or different halogen atoms;nitro; cyano; and optionally halogen-substituted phenyl and phenoxy; orrepresents cycloalkyl or cycloalkylalkyl with in each case 3 to 7 carbonatoms in the cycloalkyl part and 1 to 4 carbon atoms in the alkyl partand in each case optionally monosubstituted or polysubstituted by alkylwith 1 to 4 carbon atoms; R¹ to R⁶, which can be identical or different,represent hydrogen, straight-chain or branched alkyl with 1 to 4 carbonatoms, or represent halogenoalkyl with 1 or 2 carbon atoms and 1 to 5identical or different halogen atoms, up to a maximum of 3 substituentsrepresenting halogenoalkyl, R³ or R⁶, which can be identical ordifferent, also represent halogen, up to a maximum of 3 substituentshaving this meaning; or R¹ and R², together with the carbon atom towhich they are bonded, represent cycloalkyl which has 4 to 7 carbonatoms and is optionally substituted by alkyl with 1 or 2 carbon atoms;or R² and R³, together with the carbon atoms to which they are bonded,represent cycloalkyl which has 4 to 7 carbon atoms and is optionallysubstituted by alkyl with 1 or 2 carbon atoms,or an addition productthereof with an acid or metal salt.
 2. Anazolyl-tetrahydrofuran-2-ylidene-methane derivative or addition productaccording to claim 1, in whichR represents straight-chain or branchedalkyl with 1 to 8 carbon atoms, or represents straight-chain or branchedalkenyl or alkinyl with in each case 2 to 6 carbon atoms, or representsstraight-chain or branched alkoxyalkyl or alkylthioalkyl with in eachcase 1 to 4 carbon atoms in each alkyl part, or representshalogenoalkyl, halogenoalkoxyalkyl or halogenoalkylthioalkyl with ineach case 1 to 4 carbon atoms in each alkyl part and with in each case 1to 5 fluorine and/or chlorine atoms, or represents halogenoalkenyl with2 to 4 carbon atoms and 1 to 3 fluorine and/or chlorine atoms; orrepresents phenylalkyl, phenoxyalkyl or phenylthioalkyl with in eachcase 1 or 2 carbon atoms in the alkyl part and in each case optionallymono-, di- or tri-substituted in the phenyl part by identical ordifferent substituents selected from the group consisting of: fluorine,chlorine, methyl, ethyl, isopropyl, tert.-butyl, methoxy, methylthio,trifluoromethyl, trifluoromethoxy, trifluoromethylthio, nitro, cyano andoptionally chlorine-substituted phenyl and phenoxy; or representscyclohexyl or cyclohexylmethyl, in each case optionally substituted bymethyl and/or ethyl; R¹ to R⁶, which can be identical or different,represent hydrogen, methyl, ethyl or halogenomethyl with 1 to 3identical or different halogen atoms, a maximum of three substituentsrepresenting halogenomethyl; or R³ to R⁶, which can be identical ordifferent, also represent fluorine, chlorine or bromine, up to a maximumof three substituents having this meaning; or R¹ and R², together withthe carbon atom to which they are bonded, represent cyclopentyl orcyclohexyl; or R² and R³, together with the carbon atoms to which theyare bonded, represent cyclopentyl or cyclohexyl.
 3. A compound accordingto claim 1, wherein such compound is1-(4-chlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneof the formula ##STR135## or an addition product thereof with an acid ormetal salt.
 4. A compound according to claim 1, wherein such compound is1-cyclohexyl-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneof the formula ##STR136## or an addition product thereof with an acid ormetal salt.
 5. A compound according to claim 1, wherein such compound is1-(4-chlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(imidazol-1-yl)-ethaneof the formula ##STR137## or an addition product thereof with an acid ormetal salt.
 6. A compound according to claim 1, wherein such compound is1-(2,4-dichlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneof the formula ##STR138## or an addition product thereof with an acid ormetal salt.
 7. A compound according to claim 1, wherein such compound is1-(4-fluorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(imidazol-1-yl)-ethaneof the formula ##STR139## or an addition product thereof with an acid ormetal salt.
 8. A compound according to claim 1, wherein such compound is1-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-1-(imidazol-1-yl)-pentane ofthe formula ##STR140## or an addition product thereof with an acid ormetal salt.
 9. A compound according to claim 1, wherein such compound is1-(4-chlorophenyl)-2-(3-ethyl-3-methyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethaneof the formula ##STR141## or an addition product thereof with an acid ormetal salt.
 10. A fungicidal composition comprising a fungicidallyeffective amount of a compound or addition product thereof according toclaim 1 in admixture with a diluent.
 11. A method of combating fungiwhich comprises administering to such fungi or to a habitat thereof afungicidally effective amount of a compound or addition product thereofaccording to claim
 1. 12. The method according to claim 11, wherein suchcompoundis1-(4-chlorophenyl)-2-(3,3-dimethyl-terahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethane,1-cyclohexyl-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethane,1-(4-chlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(imidazol-1-yl)-ethane,1-(2,4-dichlorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethane,1-(4-fluorophenyl)-2-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-2-(imidazol-1-yl)-ethane,1-(3,3-dimethyl-tetrahydrofuran-2-ylidene)-1-(imidazol-1-yl)-pentane or1-(4-chlorophenyl)-2-(3-ethyl-3-methyl-tetrahydrofuran-2-ylidene)-2-(1,2,4-triazol-1-yl)-ethane,oran addition product thereof with an acid or metal salt.
 13. A method ofcombating phytopathogenic fungi which comprises applying to such fungi,to a plant or to a field in which a plant is growing or to be grown aphytopathogen fungicidally effective amount of a compound or additionproduct according to claim 1.